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Process Development Associate

4 months ago

Gaithersburg, United States Meet Full time

Meet is currently partnered with a global biopharmaceutical company focused within the vaccines development space. Our client has an extensive pipeline of clinical and commercial vaccines that impact infectious diseases across the world.


Responsibilities include but are not limited to:

• Perform scale-up of processes to deliver materials for pre-clinical and clinical studies

• Coordinate with scientist to execute optimization experiments to demonstrate that the process is robust with high purity, yield, and scalable for clinical stage manufacturing of vaccine and other biologic product candidates

• Provide reagents and other supplies for various projects and departments

• Support process characterization studies, process validation and tech transfer process as needed

• Maintaining inventory of lab supplies and ordering lab consumables as needed

• Responsible for preparation of buffers and column packing at different scales

• Performs testing of in-process samples such as SDS-PAGE, Western blot, A280 (Nanodrop), BCA, DNA, and host cell protein ELISA assays

• Performs washing and decontamination of glassware and distributing to appropriate locations within the laboratories

• Operates the glass washing instruments and autoclaves as needed

• Assists in shipping and receiving of supplies and maintaining inventory

• This position is expected to be hands on in the laboratory and scale-up operation


Minimum requirements:

• Minimum BS in relevant scientific discipline with 0-2 years of industry experience

• Downstream purification experience and knowledge is desired


Useful qualifications for the role:

• Knowledge in purification of vaccines/biologics; Experience in various chromatography methods, filtration, and TFF unit operations at bench scale and/or pilot scale is a plus

• Capable of performing multiple functions in a fast-paced environment. Strong technical protocol/report writing, and good organization skills are required

• Excellent record keeping abilities to adequately record, analyze and document data generated in support of regulatory requirements

• Demonstrated verbal and written skills in communicating scientific and technical information

• Proficient in Window based software including Excel, PowerPoint and Word